Canonical Allele Identifier: CA562773094

Gene: IL13

Linked Data

• dbSNP Id: rs1311787281
• gnomAD v2: 5-131992707-G-GT
• gnomAD v3: 5-132657015-G-GT
• gnomAD v4: 5-132657015-G-GT
• MyVariant Identifiers: chr5:g.131992707_131992708insT (hg19) ; chr5:g.132657015_132657016insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132657017dup , CM000667.2:g.132657017dup	GRCh38
NC_000005.9:g.131992709dup , CM000667.1:g.131992709dup	GRCh37
NC_000005.8:g.132020608dup	NCBI36
NG_012090.1:g.3845dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000459878.5:n.107+387dup
ENST00000468334.5:n.369-49dup
ENST00000487267.5:n.96-49dup
NM_001354991.1:c.-93+387dup	NP_001341920.1:n.-93+387dup
NM_001354992.1:c.-271-49dup	NP_001341921.1:n.-271-49dup
NM_001354993.1:c.-200-49dup	NP_001341922.1:n.-200-49dup
NM_001354991.2:c.-93+387dup	NP_001341920.1:n.-93+387dup
NM_001354992.2:c.-271-49dup	NP_001341921.1:n.-271-49dup
NM_001354993.2:c.-200-49dup	NP_001341922.1:n.-200-49dup